Canonical Allele Identifier: CA347498428

Gene: GNLY

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85697606C>G , CM000664.2:g.85697606C>G	GRCh38
NC_000002.11:g.85924729C>G , CM000664.1:g.85924729C>G	GRCh37
NC_000002.10:g.85778240C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006433.5:c.356C>G MANE Select	NP_006424.2:p.Thr119Ser
ENST00000263863.9:c.356C>G MANE Select	ENSP00000263863.5:p.Thr119Ser
NM_001302758.1:c.437C>G	NP_001289687.1:p.Thr146Ser
NM_001302758.2:c.437C>G	NP_001289687.1:p.Thr146Ser
NM_006433.4:c.356C>G	NP_006424.2:p.Thr119Ser
NM_012483.3:c.311C>G	NP_036615.2:p.Thr104Ser
NM_012483.4:c.311C>G	NP_036615.2:p.Thr104Ser
ENST00000263863.8:c.356C>G	ENSP00000263863.4:p.Thr119Ser
ENST00000409696.7:c.311C>G	ENSP00000387116.3:p.Thr104Ser
ENST00000489980.5:n.1800C>G
ENST00000524600.5:c.437C>G	ENSP00000436423.1:p.Thr146Ser
ENST00000526018.1:c.256C>G
XM_005264084.2:c.337-958C>G	XP_005264141.1:n.337-958C>G
XM_005264085.2:c.256-958C>G	XP_005264142.1:n.256-958C>G
XM_005264087.2:c.211-958C>G	XP_005264144.1:n.211-958C>G